Canonical Allele Identifier: CA425136551

Gene: APOB

Linked Data

• MyVariant Identifiers: chr2:g.21238333G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21015461G>A , CM000664.2:g.21015461G>A	GRCh38
NC_000002.11:g.21238333G>A , CM000664.1:g.21238333G>A	GRCh37
NC_000002.10:g.21091838G>A	NCBI36
NG_011793.1:g.33613C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*2723C>T	ENSP00000501110.2:n.*2723C>T
ENST00000673882.2:c.*2512C>T	ENSP00000501253.2:n.*2512C>T
ENST00000673739.1:c.3131C>T	ENSP00000501110.1:n.3131C>T
ENST00000673882.1:c.2920C>T	ENSP00000501253.1:n.2920C>T
ENST00000233242.5:c.3417C>T MANE Select	ENSP00000233242.1:p.Ala1139=
ENST00000616098.4:c.3417C>T	ENSP00000477990.1:p.Ala1139=
NM_000384.2:c.3417C>T	NP_000375.2:p.Ala1139=
XM_011532809.1:c.3417C>T	XP_011531111.1:p.Ala1139=
NM_000384.3:c.3417C>T MANE Select	NP_000375.3:p.Ala1139=